free energy

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free energy

The Columbia Encyclopedia, Sixth Edition | 2008 | The Columbia Encyclopedia, Sixth Edition. Copyright 2008 Columbia University Press. (Hide copyright information) Copyright

free energy or Gibbs free energy, quantity derived from the relationships between heat and work studied in thermodynamics and used as a measure of the relative stability of a physical or chemical system, i.e., the tendency of the system to react or change. If the change in free energy, Δ G, is negative, the transformation of the system will occur spontaneously, since transitions in which the energy decreases are favored, whereas those in which it increases (Δ G positive) are not. The change in free energy for a given process at a particular temperature depends on three factors, as seen from the equation Δ G = Δ H - T Δ S, where Δ H is the change in the enthalpy of the system, T is the temperature in degrees Kelvin, and Δ S is the change in entropy . A negative value of the enthalpy change indicates a decrease in the heat content of the system and contributes to a favorable value of the free energy; a positive entropy change indicates a decrease in the orderliness of the system and also contributes to a favorable value of the free energy, since a system tends to go from more ordered to less ordered states. It may happen that the change in enthalpy for the reaction is favorable but that of the entropy is unfavorable, or vice versa; in such a case the temperature is the deciding factor since it determines how much weight is given to the entropy change. For example, in the transition of liquid water to ice, the enthalpy change is favorable because heat is released in the process but the entropy change is unfavorable because the transition is to the more ordered, crystalline state. Below a temperature of 32°F (273°K) the enthalpy term, Δ H, is larger and the process is spontaneous, but at higher temperatures the entropy term, T Δ S, predominates, and the transition does not occur. Although the free energy indicates whether or not a given reaction will occur, it gives no information about the speed of such a reaction. The reaction of hydrogen with oxygen to form water has a favorable, negative, free energy, but the reaction rate is so slow that without the presence of a catalyst it is not observable. Scientists use tables listing the standard free energy, Δ G °, of various compounds; the standard free energy is the change in free energy when one mole of the compound is formed at 25°C and 1 atmospheric pressure.

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"free energy." The Columbia Encyclopedia, Sixth Edition. 2008. Encyclopedia.com. 14 Nov. 2009 <http://www.encyclopedia.com>.

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Gibbs free energy

A Dictionary of Earth Sciences | 1999 | | © A Dictionary of Earth Sciences 1999, originally published by Oxford University Press 1999. (Hide copyright information) Copyright

Gibbs free energy See GIBBS FUNCTION.

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AILSA ALLABY and MICHAEL ALLABY. "Gibbs free energy." A Dictionary of Earth Sciences. 1999. Encyclopedia.com. 14 Nov. 2009 <http://www.encyclopedia.com>.

AILSA ALLABY and MICHAEL ALLABY. "Gibbs free energy." A Dictionary of Earth Sciences. 1999. Encyclopedia.com. (November 14, 2009). http://www.encyclopedia.com/doc/1O13-Gibbsfreeenergy.html

AILSA ALLABY and MICHAEL ALLABY. "Gibbs free energy." A Dictionary of Earth Sciences. 1999. Retrieved November 14, 2009 from Encyclopedia.com: http://www.encyclopedia.com/doc/1O13-Gibbsfreeenergy.html

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free energy

A Dictionary of Biology | 2004 | © A Dictionary of Biology 2004, originally published by Oxford University Press 2004. (Hide copyright information) Copyright

free energy A measure of a system's ability to do work. The Gibbs free energy (or Gibbs function), G, is defined by G = HTS, where G is the energy liberated or absorbed in a reversible process at constant pressure and constant temperature (T), H is the enthalpy and S the entropy of the system. Changes in Gibbs free energy, ΔG, are useful in indicating the conditions under which a chemical reaction will occur. If ΔG is positive the reaction will only occur if energy is supplied to force it away from the equilibrium position (i.e. when ΔG = 0). If ΔG is negative the reaction will proceed spontaneously to equilibrium.

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